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Whether these rapid responses reflect true biological effects or placebo components remains difficult to distinguish

McFarlane called the approval of Miplyffa a monumental milestone for NPC patients and their family members in the U.S

The most likely timeline points to a potential FDA approval in late the next year, with commercial availability following shortly after

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The dose ceiling of 2.4 mg represents the point where increasing the dose further produces diminishing returns with escalating gastrointestinal problems

Thymosin 4 and a synthetic peptide containing its actin-binding domain promote dermal wound repair in db/db diabetic mice and in aged mice